Brugada syndrome (BrS) remains genetically heterogeneous and is associated with slowed cardiac conduction. We aimed to identify genetic variation in BrS cases at loci associated with QRS duration.
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study
TORCHIO, MARGHERITA;DAGRADI, FEDERICA;SCHWARTZ, PETER;CROTTI, LIA;
2015-01-01
Abstract
Brugada syndrome (BrS) remains genetically heterogeneous and is associated with slowed cardiac conduction. We aimed to identify genetic variation in BrS cases at loci associated with QRS duration.File in questo prodotto:
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